TY - JOUR
T1 - Bone Regeneration in A Large Animal Model Featuring A Modular Off-The-Shelf Soft Callus Mimetic
AU - de Silva, Leanne
AU - Longoni, Alessia
AU - Staubli, Flurina
AU - Nurmohamed, Silke
AU - Duits, Anneli
AU - Rosenberg, Antoine Jwp
AU - Gawlitta, Debby
N1 - Funding Information:
The goats were part of the MACRON project under number AOCMF‐17‐17G from the AO Foundation. The antibody against collagen type II (II‐II6B3), developed by T.F. Linsenmayer, was obtained from the DSHB developed under the auspices of the NICHD and maintained by The University of Iowa, Department of Biology, Iowa City, IA52242. We highly appreciate the discussions on the animal model with Prof. Moyo Kruijt. LdS was supported by the Marie Skłodowska‐Curie Actions (Grant agreement RESCUE #801540).
Publisher Copyright:
© 2023 The Authors. Advanced Healthcare Materials published by Wiley-VCH GmbH.
PY - 2023/11/22
Y1 - 2023/11/22
N2 - Implantation of engineered cartilage with soft callus features triggers remodeling to bone tissue via endochondral bone regeneration (EBR). Thus far, EBR has not progressed to the level of large animals on the axis of clinical translation. Herein, the feasibility of EBR is aimed for a critical-sized defect in a large animal model. Chondrogenesis is first induced in goat-derived multipotent mesenchymal stromal cells (MSCs) by fine-tuning the cellular differentiation process. Through a unique devitalization process, two off-the-shelf constructs aimed to recapitulate the different stages of the transient cartilaginous soft callus template in EBR are generated. To evaluate bone regeneration, the materials are implanted in an adapted bilateral iliac crest defect model in goats, featuring a novel titanium star-shaped spacer. After 3 months, the group at the more advanced differentiation stage shows remarkable regenerative capacity, with comparable amounts of bone regeneration as the autograft group. In contrast, while the biomaterial mimicking the earlier stages of chondrogenesis shows improved regeneration compared to the negative controls, this is subpar compared to the more advanced material. Concluding, EBR is attainable in large animals with a soft callus mimetic material that leads to fast conversion into centimeter-scale bone, which prospects successful implementation in the human clinics.
AB - Implantation of engineered cartilage with soft callus features triggers remodeling to bone tissue via endochondral bone regeneration (EBR). Thus far, EBR has not progressed to the level of large animals on the axis of clinical translation. Herein, the feasibility of EBR is aimed for a critical-sized defect in a large animal model. Chondrogenesis is first induced in goat-derived multipotent mesenchymal stromal cells (MSCs) by fine-tuning the cellular differentiation process. Through a unique devitalization process, two off-the-shelf constructs aimed to recapitulate the different stages of the transient cartilaginous soft callus template in EBR are generated. To evaluate bone regeneration, the materials are implanted in an adapted bilateral iliac crest defect model in goats, featuring a novel titanium star-shaped spacer. After 3 months, the group at the more advanced differentiation stage shows remarkable regenerative capacity, with comparable amounts of bone regeneration as the autograft group. In contrast, while the biomaterial mimicking the earlier stages of chondrogenesis shows improved regeneration compared to the negative controls, this is subpar compared to the more advanced material. Concluding, EBR is attainable in large animals with a soft callus mimetic material that leads to fast conversion into centimeter-scale bone, which prospects successful implementation in the human clinics.
KW - critical-sized defects
KW - devitalization
KW - endochondral bone tissue regeneration
KW - large animal models
KW - mesenchymal stromal cells
UR - http://www.scopus.com/inward/record.url?scp=85168616522&partnerID=8YFLogxK
U2 - 10.1002/adhm.202301717
DO - 10.1002/adhm.202301717
M3 - Article
C2 - 37580174
SN - 2192-2659
VL - 12
JO - Advanced Healthcare Materials
JF - Advanced Healthcare Materials
IS - 29
M1 - 2301717
ER -